Ultrafast Directional Janus Pt-Mesoporous Silica Nanomotors for Smart Drug Delivery

被引:118
作者
Diez, Paula [1 ,2 ,3 ]
Lucena-Sanchez, Elena [1 ,2 ,3 ]
Escudero, Andrea [1 ,2 ,3 ]
Llopis-Lorente, Antoni [1 ,2 ,3 ]
Villalonga, Reynaldo [4 ]
Martinez-Manez, Ramon [1 ,2 ,3 ,5 ]
机构
[1] Univ Politecn Valencia, Univ Valencia, Inst Interuniv Invest Reconocimiento Mol & Desarr, Valencia 46022, Spain
[2] Univ Politecn Valencia, Unidad Mixta UPV CIPF Invest Mecanismos Enfermeda, Valencia 46012, Spain
[3] CIBER Bioingn Biomat & Nanomed CIBER BBN, Madrid 28029, Spain
[4] Univ Complutense Madrid, Fac Chem, Dept Analyt Chem, Nanosensors & Nanomachines Grp, Madrid 28040, Spain
[5] Univ Politecn Valencia, Unidad Mixta Invest Nanomed & Sensores, Inst Invest Sanitaria La Fe, Valencia 46026, Spain
关键词
Janus nanomotors; directional motion; ultrafast self-propulsion; drug delivery; on-command controlled release;
D O I
10.1021/acsnano.0c08404
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Development of bioinspired nanomachines with an efficient propulsion and cargo-towing has attracted much attention in the last years due to their potential biosensing, diagnostics, and therapeutics applications. In this context, self-propelled synthetic nanomotors are promising carriers for intelligent and controlled release of therapeutic payloads. However, the implementation of this technology in real biomedical applications is still facing several challenges. Herein, we report the design, synthesis, and characterization of innovative multifunctional gated platinum-mesoporous silica nanomotors constituted of a propelling element (platinum nanodendrite face), a drug-loaded nanocontainer (mesoporous silica nanoparticle face), and a disulfide-containing oligo(ethylene glycol) chain (S-S-PEG) as a gating system. These Janus-type nanomotors present an ultrafast self-propelled motion due to the catalytic decomposition of low concentrations of hydrogen peroxide. Likewise, nanomotors exhibit a directional movement, which drives the engines toward biological targets, THP-1 cancer cells, as demonstrated using a microchip device that mimics penetration from capillary to postcapillary vessels. This fast and directional displacement facilitates the rapid cellular internalization and the on-demand specific release of a cytotoxic drug into the cytosol, due to the reduction of the disulfide bonds of the capping ensemble by intracellular glutathione levels. In the microchip device and in the absence of fuel, nanomotors are neither able to move directionally nor reach cancer cells and deliver their cargo, revealing that the fuel is required to get into inaccessible areas and to enhance nanoparticle internalization and drug release. Our proposed nanosystem shows many of the suitable characteristics for ideal biomedical destined nanomotors, such as rapid autonomous motion, versatility, and stimuli-responsive controlled drug release.
引用
收藏
页码:4467 / 4480
页数:14
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